H.R.4829 - Reducing Fraudulent and Imitation Drugs Act of 2006109th Congress (2005-2006)
|Sponsor:||Rep. Burton, Dan [R-IN-5] (Introduced 03/01/2006)|
|Committees:||House - Energy and Commerce|
|Latest Action:||03/17/2006 Referred to the Subcommittee on Health.|
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Summary: H.R.4829 — 109th Congress (2005-2006)All Bill Information (Except Text)
Introduced in House (03/01/2006)
Reducing Fraudulent and Imitation Drugs Act of 2006 - Directs the Secretary of Health and Human Services to require prescription drug packaging to incorporate: (1) radio frequency tagging technology or similar trace and track technologies; (2) tamper-indicating technologies; and (3) blister security packaging when possible.
Directs the Secretary to: (1) require that such technologies be used exclusively to authenticate the pedigree of prescription drugs; and (2) prohibit such technologies from containing or transmitting any identifying information of a health care practitioner or consumer, or any advertisement or information about indications or off-label uses.Requires the Secretary to encourage prescription drug manufacturers and distributors to incorporate: (1) overt optically variable counterfeit-resistant technologies into packaging; and (2) required prescription drug packaging technologies into multiple elements of the physical packaging of the drugs. Requires prescription drug shipments to include a label on the shipping container that incorporates packaging technologies.
Deems a prescription drug to be misbranded if the packaging or labeling of the drug is in violation of a requirement or prohibition of this Act.
Requires the Secretary to publish the National Specified List of Susceptible Prescription Drugs, consisting of not less than 30 of the most frequently counterfeited prescription drugs in the United States.